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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5966556insertion1nstd209human GRCh38 chr4: 145,768,890-145,768,890 , GRCh37.p13 chr4: 146,690,042-146,690,042 C4orf51, ZNF827
    nsv5953795insertion1nstd209human GRCh38 chr4: 145,848,590-145,848,590 , GRCh37.p13 chr4: 146,769,742-146,769,742 ZNF827
    nsv5900391copy number variation1nstd209human GRCh38 chr4: 145,806,402-145,807,715 , GRCh37.p13 chr4: 146,727,554-146,728,867 ZNF827
    nsv5899444copy number variation1nstd209human GRCh38 chr4: 145,832,668-145,838,159 , GRCh37.p13 chr4: 146,753,820-146,759,311 ZNF827
    nsv5895314copy number variation1nstd209human GRCh38 chr4: 145,848,922-145,849,142 , GRCh37.p13 chr4: 146,770,074-146,770,294 ZNF827
    nsv5889383copy number variation1nstd209human GRCh38 chr4: 145,826,765-145,826,814 , GRCh37.p13 chr4: 146,747,917-146,747,966 ZNF827
    nsv5838045copy number variation1nstd209human GRCh38 chr4: 145,832,685-145,838,036 , GRCh37.p13 chr4: 146,753,837-146,759,188 ZNF827
    nsv5691349mobile element insertion1nstd211human GRCh38 chr4: 145,897,820-145,897,820 , GRCh37.p13 chr4: 146,818,972-146,818,972 ZNF827
    nsv5689616mobile element insertion1nstd211human GRCh38 chr4: 145,818,430-145,818,430 , GRCh37.p13 chr4: 146,739,582-146,739,582 ZNF827
    nsv5688272mobile element insertion1nstd211human GRCh38 chr4: 145,863,600-145,863,600 , GRCh37.p13 chr4: 146,784,752-146,784,752 ZNF827
    nsv5680103mobile element insertion2nstd211human GRCh38 chr4: 145,892,686-145,892,686 , GRCh37.p13 chr4: 146,813,838-146,813,838 ZNF827
    nsv5674919mobile element insertion1nstd211human GRCh38 chr4: 145,764,097-145,764,097 , GRCh37.p13 chr4: 146,685,249-146,685,249 C4orf51, ZNF827
    nsv5623844insertion1nstd207human GRCh38 chr4: 145,826,765-145,826,765 , GRCh37.p13 chr4: 146,747,917-146,747,917 ZNF827
    nsv5621132insertion1nstd207human GRCh38 chr4: 145,793,328-145,793,328 , GRCh37.p13 chr4: 146,714,480-146,714,480 ZNF827
    nsv5610924insertion1nstd207human GRCh38 chr4: 145,892,670-145,892,670 , GRCh37.p13 chr4: 146,813,822-146,813,822 ZNF827
    nsv5579016copy number variation1nstd207human GRCh38 chr4: 145,846,370-145,846,708 , GRCh37.p13 chr4: 146,767,522-146,767,860 ZNF827
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5545800insertion1nstd206human GRCh38 chr4: 145,826,753-145,826,765 , GRCh37.p13 chr4: 146,747,905-146,747,917 ZNF827
    nsv5541863insertion1nstd206human GRCh38 chr4: 145,793,338-145,793,379 , GRCh37.p13 chr4: 146,714,490-146,714,531 ZNF827
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